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N-(4-Carbethoxyphenyl)maleamic acid is a chemical compound that is formed through the reaction of maleamic acid and 4-Carbethoxyaniline. It is known for its compositional stability and reactivity, making it a valuable substance in the field of chemistry. However, the toxicity and potential risks associated with this compound are yet to be fully understood. As with most chemicals, it is essential to handle N-(4-Carbethoxyphenyl)maleamic acid with care and adhere to standard safety protocols in a laboratory environment.

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  • Benzoicacid, 4-[(3-carboxy-1-oxo-2-propen-1-yl)amino]-, 1-ethyl ester

    Cas No: 200126-82-5

  • USD $ 1.9-2.9 / Gram

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  • 200126-82-5 Structure
  • Basic information

    1. Product Name: N-(4-CARBETHOXYPHENYL)MALEAMIC ACID
    2. Synonyms: ASISCHEM D13253;OTAVA-BB BB7010590141;N-(4-ETHOXYCARBONYLPHENYL)MALEAMIC ACID;N-(4-CARBETHOXYPHENYL)MALEAMIC ACID;n-(4-carboethoxyphenyl)maleamic acid;4-{[4-(Ethoxycarbonyl)phenyl]amino}-4-oxobut-2-enoic acid
    3. CAS NO:200126-82-5
    4. Molecular Formula: C13H13NO5
    5. Molecular Weight: 263.25
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 200126-82-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 506.7 °C at 760 mmHg
    3. Flash Point: 260.2 °C
    4. Appearance: /
    5. Density: 1.328 g/cm3
    6. Vapor Pressure: 4.35E-11mmHg at 25°C
    7. Refractive Index: 1.6
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N-(4-CARBETHOXYPHENYL)MALEAMIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-(4-CARBETHOXYPHENYL)MALEAMIC ACID(200126-82-5)
    12. EPA Substance Registry System: N-(4-CARBETHOXYPHENYL)MALEAMIC ACID(200126-82-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 36/37/38
    3. Safety Statements: 26-36
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 200126-82-5(Hazardous Substances Data)

200126-82-5 Usage

Uses

Used in Chemical Research:
N-(4-Carbethoxyphenyl)maleamic acid is used as a research compound for various chemical studies. Its unique properties, such as stability and reactivity, make it a valuable tool in understanding chemical reactions and processes.
Used in Laboratory Procedures:
Due to its compositional stability and reactivity, N-(4-Carbethoxyphenyl)maleamic acid is employed in various laboratory procedures. It can be utilized in the synthesis of other compounds or as a reagent in chemical reactions, contributing to the advancement of chemical knowledge and applications.
Used in Pharmaceutical Development:
Although its toxicity and potential risks are not yet fully determined, N-(4-Carbethoxyphenyl)maleamic acid may have potential applications in the pharmaceutical industry. Its unique chemical properties could be harnessed for the development of new drugs or as an intermediate in the synthesis of pharmaceutical compounds.
Used in Material Science:
N-(4-Carbethoxyphenyl)maleamic acid's properties may also be relevant in material science, where it could be used in the development of new materials or as a component in the synthesis of advanced materials with specific properties. Its stability and reactivity could contribute to the creation of materials with unique characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 200126-82-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,1,2 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 200126-82:
(8*2)+(7*0)+(6*0)+(5*1)+(4*2)+(3*6)+(2*8)+(1*2)=65
65 % 10 = 5
So 200126-82-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H13NO5/c1-2-19-13(18)9-3-5-10(6-4-9)14-11(15)7-8-12(16)17/h3-8H,2H2,1H3,(H,14,15)(H,16,17)/b8-7-

200126-82-5 Well-known Company Product Price

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  • Alfa Aesar

  • (B25298)  N-(4-Ethoxycarbonylphenyl)maleamic acid, 97%   

  • 200126-82-5

  • 5g

  • 401.0CNY

  • Detail
  • Alfa Aesar

  • (B25298)  N-(4-Ethoxycarbonylphenyl)maleamic acid, 97%   

  • 200126-82-5

  • 25g

  • 1609.0CNY

  • Detail
  • Alfa Aesar

  • (B25298)  N-(4-Ethoxycarbonylphenyl)maleamic acid, 97%   

  • 200126-82-5

  • 100g

  • 5247.0CNY

  • Detail

200126-82-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-ethoxycarbonylanilino)-4-oxobut-2-enoic acid

1.2 Other means of identification

Product number -
Other names N-(4-Ethoxycarbonylphenyl)maleamic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:200126-82-5 SDS

200126-82-5Relevant articles and documents

Synthesis of Diels-Alder adducts of N-arylmaleimides by a multicomponent reaction between maleic anhydride, dienes, and anilines

Guevara-Salazar, J. Alberto,Quintana-Zavala, Delia,Jimenez-Vazquez, Hugo A.,Trujillo-Ferrara, Jose

experimental part, p. 827 - 836 (2012/07/27)

We have carried out the synthesis and characterization of some hexahydroisoindolyl benzoic acids and their corresponding ethyl esters by a multicomponent reaction (MCR) between aminobenzoic acids or aminobenzoates, maleic anhydride, and isoprene in the ab

4-(3-Dialkylamino-2,5-dioxopyrrolidin-1-yl)benzoic acid esters

Kolyamshin,Danilov,Kol'Tsov

, p. 393 - 396 (2007/10/03)

Reactions of alkyl 4-aminobenzoates with maleic anhydride give the corresponding alkyl 4-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)benzoates, and the latter are converted into 4-(3-dialkylamino-2,5-dioxo-2,3,4,5-tetrahydro-1H- pyrrol-1-yl)benzoates by treatme

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